DK2311879T3 - Monoclonal antibodies to claudin-18 for the treatment of cancer - Google Patents
Monoclonal antibodies to claudin-18 for the treatment of cancer Download PDFInfo
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- DK2311879T3 DK2311879T3 DK10011776.1T DK10011776T DK2311879T3 DK 2311879 T3 DK2311879 T3 DK 2311879T3 DK 10011776 T DK10011776 T DK 10011776T DK 2311879 T3 DK2311879 T3 DK 2311879T3
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EP05025657A EP1790664A1 (en) | 2005-11-24 | 2005-11-24 | Monoclonal antibodies against claudin-18 for treatment of cancer |
EP06818817A EP1948693B1 (en) | 2005-11-24 | 2006-11-24 | Monoclonal antibodies against claudin-18 for treatment of cancer |
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DK10011776.1T DK2311879T3 (en) | 2005-11-24 | 2006-11-24 | Monoclonal antibodies to claudin-18 for the treatment of cancer |
DK10011775.3T DK2311878T3 (en) | 2005-11-24 | 2006-11-24 | Monoclonal antibodies to Claudin-18 for the treatment of cancer |
DK19202848.8T DK3656793T3 (da) | 2005-11-24 | 2006-11-24 | Monoklonale antistoffer mod claudin-18 til cancerbehandling |
DK06818817.6T DK1948693T3 (da) | 2005-11-24 | 2006-11-24 | Monoklonale antistoffer mod claudin-18 til behandling af cancer |
DK10011772.0T DK2325210T3 (en) | 2005-11-24 | 2006-11-24 | MONOCLONAL ANTIBODIES AGAINST CLAUDIN-18 FOR CANCER TREATMENT |
DK17192466T DK3312197T3 (da) | 2005-11-24 | 2006-11-24 | Monoklonale antistoffer mod claudin-18 til behandling af cancer |
DK10011773.8T DK2311877T3 (en) | 2005-11-24 | 2006-11-24 | Monoclonal antibodies to claudin-18 for treating cancer |
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DK10011775.3T DK2311878T3 (en) | 2005-11-24 | 2006-11-24 | Monoclonal antibodies to Claudin-18 for the treatment of cancer |
DK19202848.8T DK3656793T3 (da) | 2005-11-24 | 2006-11-24 | Monoklonale antistoffer mod claudin-18 til cancerbehandling |
DK06818817.6T DK1948693T3 (da) | 2005-11-24 | 2006-11-24 | Monoklonale antistoffer mod claudin-18 til behandling af cancer |
DK10011772.0T DK2325210T3 (en) | 2005-11-24 | 2006-11-24 | MONOCLONAL ANTIBODIES AGAINST CLAUDIN-18 FOR CANCER TREATMENT |
DK17192466T DK3312197T3 (da) | 2005-11-24 | 2006-11-24 | Monoklonale antistoffer mod claudin-18 til behandling af cancer |
DK10011773.8T DK2311877T3 (en) | 2005-11-24 | 2006-11-24 | Monoclonal antibodies to claudin-18 for treating cancer |
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Families Citing this family (122)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE10254601A1 (de) * | 2002-11-22 | 2004-06-03 | Ganymed Pharmaceuticals Ag | Differentiell in Tumoren exprimierte Genprodukte und deren Verwendung |
DE102004024617A1 (de) | 2004-05-18 | 2005-12-29 | Ganymed Pharmaceuticals Ag | Differentiell in Tumoren exprimierte Genprodukte und deren Verwendung |
CA2573430C (en) * | 2004-06-07 | 2015-02-24 | Kyowa Hakko Kogyo Co., Ltd. | Anti-perp antibody |
EP1790664A1 (en) | 2005-11-24 | 2007-05-30 | Ganymed Pharmaceuticals AG | Monoclonal antibodies against claudin-18 for treatment of cancer |
CA2632419A1 (en) * | 2005-12-06 | 2007-06-14 | Kyowa Hakko Kogyo Co., Ltd. | Genetically recombinant anti-perp antibody |
EP1997832A1 (en) * | 2007-05-29 | 2008-12-03 | Ganymed Pharmaceuticals AG | Monoclonal antibodies against Claudin-18 for treatment of cancer |
US8846036B2 (en) * | 2007-10-19 | 2014-09-30 | Abbott Laboratories | Antibodies that bind to mammalian NGAL and uses thereof |
US20090124022A1 (en) * | 2007-10-19 | 2009-05-14 | Abbott Laboratories | Antibodies that bind to mammalian ngal and uses thereof |
US20090123946A1 (en) * | 2007-10-19 | 2009-05-14 | Abbott Laboratories | Immunoassays and kits for the detection of ngal |
FI2398902T3 (fi) | 2009-02-20 | 2023-11-28 | Astellas Pharma Inc | Menetelmiä ja koostumuksia syövän diagnoosia ja hoitoa varten |
KR102126964B1 (ko) | 2009-11-11 | 2020-06-25 | 가니메드 파마슈티칼스 게엠베하 | 클라우딘 6 특이적 항체 |
DK2504363T3 (da) | 2009-11-24 | 2019-07-29 | Alethia Biotherapeutics Inc | Anti-clusterin-antistoffer og antigenbindende fragmenter og deres anvendelse til reducering af tumorvolumen |
KR20220017432A (ko) | 2010-02-24 | 2022-02-11 | 이뮤노젠 아이엔씨 | 엽산염 수용체 1 항체와 면역접합체 및 이들의 용도 |
EP2404936A1 (en) * | 2010-07-06 | 2012-01-11 | Ganymed Pharmaceuticals AG | Cancer therapy using CLDN6 target-directed antibodies in vivo |
JP5995851B2 (ja) * | 2010-10-18 | 2016-09-21 | メディアファーマ エス. アール. エル.Mediapharma S. R. L. | ErbB3結合抗体 |
EP2663579B1 (en) | 2011-01-14 | 2017-04-26 | The Regents of the University of California | Therapeutic antibodies against ror-1 protein and methods for use of same |
EP2668210B1 (en) | 2011-01-26 | 2020-06-17 | Celldex Therapeutics, Inc. | Anti-kit antibodies and uses thereof |
ES2683953T3 (es) * | 2011-02-07 | 2018-09-28 | Aggamin Llc | Procedimientos y sistemas para tratar o prevenir trastornos hipertensivos gestacionales |
US8722044B2 (en) * | 2011-03-15 | 2014-05-13 | Janssen Biotech, Inc. | Human tissue factor antibody and uses thereof |
CA3182262A1 (en) | 2011-04-01 | 2012-10-04 | Immunogen, Inc. | Methods for increasing efficacy of folr1 cancer therapy |
DK3026064T3 (en) * | 2011-05-13 | 2019-01-14 | Ganymed Pharmaceuticals Gmbh | ANTIBODIES FOR TREATMENT OF CANCER EXPRESSING CLAUDIN 6 |
CA3234629A1 (en) | 2011-12-20 | 2013-06-27 | Janssen Biotech, Inc. | Anti-phf-tau antibodies and their uses |
EP2817028A4 (en) | 2012-02-22 | 2015-11-04 | Alethia Biotherapeutics Inc | COMMON USE OF A CLUSTERIN INHIBITOR AND EGFR INHIBITOR FOR TREATING CANCER |
WO2013167153A1 (en) * | 2012-05-09 | 2013-11-14 | Ganymed Pharmaceuticals Ag | Antibodies useful in cancer diagnosis |
WO2013174403A1 (en) * | 2012-05-23 | 2013-11-28 | Ganymed Pharmaceuticals Ag | Combination therapy involving antibodies against claudin 18.2 for treatment of cancer |
EP3725810B1 (en) | 2012-05-23 | 2022-07-06 | Astellas Pharma Inc. | Combination therapy involving antibodies against claudin 18.2 for treatment of cancer |
WO2013174404A1 (en) | 2012-05-23 | 2013-11-28 | Ganymed Pharmaceuticals Ag | Combination therapy involving antibodies against claudin 18.2 for treatment of cancer |
SG11201500489YA (en) | 2012-07-25 | 2015-02-27 | Kolltan Pharmaceuticals Inc | Anti-kit antibodies and uses thereof |
SG10201804260QA (en) | 2012-08-31 | 2018-07-30 | Immunogen Inc | Diagnostic assays and kits for detection of folate receptor 1 |
BR122020024124B1 (pt) * | 2012-11-13 | 2024-01-30 | Biontech Ag | Agentes para tratamento de doenças cancerosas expressando claudina |
CA2890438C (en) * | 2012-11-13 | 2022-10-18 | Biontech Ag | Agents for treatment of claudin expressing cancer diseases |
CA2895508A1 (en) | 2012-12-18 | 2014-06-26 | Icahn School Of Medicine At Mount Sinai | Influenza virus vaccines and uses thereof |
EP4177273A1 (en) * | 2013-02-20 | 2023-05-10 | Astellas Pharma Inc. | Combination therapy involving antibodies against claudin 18.2 for treatment of cancer |
WO2014127785A1 (en) * | 2013-02-20 | 2014-08-28 | Ganymed Pharmaceuticals Ag | Combination therapy involving antibodies against claudin 18.2 for treatment of cancer |
WO2014159531A1 (en) * | 2013-03-14 | 2014-10-02 | The Board Of Regents Of The University Of Texas System | Monoclonal antibodies targeting epcam for detection of prostate cancer lymph node metastases |
WO2014159960A1 (en) | 2013-03-14 | 2014-10-02 | Icahn School Of Medicine At Mount Sinai | Antibodies against influenza virus hemagglutinin and uses thereof |
SI2976360T1 (sl) * | 2013-03-18 | 2020-04-30 | Astellas Pharma Inc. | Terapija, ki vključuje protitelesa proti Klavdinu 18.2 za zdravljenje raka |
WO2014146672A1 (en) * | 2013-03-18 | 2014-09-25 | Ganymed Pharmaceuticals Ag | Therapy involving antibodies against claudin 18.2 for treatment of cancer |
WO2015014376A1 (en) | 2013-07-31 | 2015-02-05 | Biontech Ag | Diagnosis and therapy of cancer involving cancer stem cells |
SG10201907501QA (en) | 2013-08-30 | 2019-10-30 | Immunogen Inc | Antibodies and assays for detection of folate receptor 1 |
RU2016122041A (ru) | 2013-11-06 | 2017-12-11 | ЭББВИ СТЕМСЕНТРКС ЭлЭлСи | Новые анти-клаудин антитела и способы их применения |
CN113908269A (zh) | 2014-05-23 | 2022-01-11 | 塞尔德克斯医疗公司 | 嗜酸性粒细胞或肥大细胞相关病症的治疗 |
JP6893594B2 (ja) * | 2014-07-10 | 2021-06-23 | ハイバーセル,インク. | 腫瘍微小環境に影響する抗癌剤と組み合わせたβ−グルカン |
CN105315375B (zh) * | 2014-07-17 | 2021-04-23 | 恺兴生命科技(上海)有限公司 | 靶向cld18a2的t淋巴细胞及其制备方法和应用 |
JP2018504412A (ja) | 2015-01-23 | 2018-02-15 | アイカーン スクール オブ メディシン アット マウント サイナイ | インフルエンザウイルスワクチン接種レジメン |
WO2016180468A1 (en) * | 2015-05-11 | 2016-11-17 | Biontech Cell & Gene Therapies Gmbh | Claudin-18.2-specific immunoreceptors and t cell epitopes |
JP6768011B2 (ja) * | 2015-06-23 | 2020-10-14 | バイエル ファーマ アクチエンゲゼルシャフト | キネシンスピンドルタンパク質(ksp)阻害剤の抗cd123抗体との抗体薬物複合体 |
CA2996522A1 (en) * | 2015-08-25 | 2017-03-02 | The Uab Research Foundation | Methods for stem cell transplantation |
CN108601828B (zh) | 2015-09-17 | 2023-04-28 | 伊缪诺金公司 | 包含抗folr1免疫缀合物的治疗组合 |
CN109310781B (zh) | 2016-06-15 | 2024-06-18 | 拜耳制药股份公司 | 具有ksp抑制剂和抗-cd123-抗体的特异性抗体-药物-缀合物(adc) |
US11266734B2 (en) | 2016-06-15 | 2022-03-08 | Icahn School Of Medicine At Mount Sinai | Influenza virus hemagglutinin proteins and uses thereof |
CN109414492A (zh) * | 2016-06-16 | 2019-03-01 | 小利兰斯坦福大学理事会 | 针对cd81的人源化和嵌合单克隆抗体 |
JP2019531084A (ja) | 2016-07-08 | 2019-10-31 | カースゲン セラピューティクス カンパニー リミテッドCarsgen Therapeutics Co., Ltd. | 抗クローディンタンパク質18a2の抗体及びその応用 |
EP3558387B1 (de) | 2016-12-21 | 2021-10-20 | Bayer Pharma Aktiengesellschaft | Spezifische antikörper-wirkstoff-konjugate (adcs) mit ksp-inhibitoren |
JP7066714B2 (ja) | 2016-12-21 | 2022-05-13 | バイエル・ファルマ・アクティエンゲゼルシャフト | 酵素的に切断可能な基を有する抗体薬物コンジュゲート(adc) |
JOP20180021A1 (ar) | 2017-03-16 | 2019-01-30 | Janssen Biotech Inc | الأجسام المضادة لتكتلات خيوط بروتين تاو (tau) الحلزونية المزدوجة واستخداماتها |
CA3058652A1 (en) * | 2017-04-07 | 2018-10-11 | Icahn School Of Medicine At Mount Sinai | Anti-influenza b virus neuraminidase antibodies and uses thereof |
EA202092122A1 (ru) * | 2018-03-08 | 2020-12-03 | Фейнз Терапьютикс, Инк. | Антитела против tip-1 и их применения |
EP3762031A4 (en) * | 2018-03-08 | 2021-12-22 | Phanes Therapeutics, Inc. | ANTI-CLAUDINE ANTIBODIES 18.2 AND THEIR USES |
KR102340989B1 (ko) | 2018-03-28 | 2021-12-20 | 에이비온 주식회사 | 클라우딘 3의 ecl-2에 특이적으로 결합하는 항체, 이의 단편 및 이들의 용도 |
CN108517315B (zh) * | 2018-03-30 | 2019-06-04 | 四川迈克生物新材料技术有限公司 | 抗人IgM单克隆抗体、其杂交瘤细胞株及应用 |
EP3794037A4 (en) * | 2018-05-18 | 2022-03-02 | Lanova Medicines Limited Company | ANTI-CLAUDIN 18.2 ANTIBODIES AND USES THEREOF |
JP7513605B2 (ja) * | 2018-07-18 | 2024-07-09 | アスクジーン・ファーマ・インコーポレイテッド | 新規な抗体ならびにそれを調製および使用するための方法 |
AU2019309948A1 (en) * | 2018-07-23 | 2021-02-25 | Boehringer Ingelheim Pharmaceuticals, Inc. | Antibodies targeting a complex comprising non-classical HLA-I and neoantigen and their methods of use |
CN112654638B (zh) * | 2018-08-27 | 2022-12-30 | 南京圣和药业股份有限公司 | 一种抗Claudin18.2抗体及其应用 |
MX2021004588A (es) | 2018-10-22 | 2022-01-18 | Shanghai Genbase Biotechnology Co Ltd | Anticuerpo anti-cldn18.2 y sus usos. |
BR112021011014A2 (pt) * | 2018-12-07 | 2021-08-31 | Zlip Holding Limited | Anticorpos anti-claudina e usos destes |
US20230192840A1 (en) * | 2018-12-28 | 2023-06-22 | Sichuan Kelun-Biotech Biopharmaceutical Co., Ltd. | Antibody and use thereof |
CN113227135A (zh) * | 2018-12-28 | 2021-08-06 | 斯帕克斯治疗公司 | 用于治疗癌症和其他疾病的对紧密连接蛋白18.2具有特异性的结合分子、其组合物和方法 |
BR112021012608A2 (pt) * | 2018-12-28 | 2021-09-08 | Nanjing GenScript Biotech Co., Ltd. | Porção de ligação que se liga especificamente à claudina18.2, receptor de antígeno quimérico, ácido nucleico, célula imune manipulada, composição farmacêutica, e, método de tratamento de um tumor ou câncer que expressa claudina18.2 |
CN111434692B (zh) * | 2019-01-15 | 2021-12-31 | 浙江道尔生物科技有限公司 | 抗cld18a2纳米抗体及其应用 |
CN109762067B (zh) * | 2019-01-17 | 2020-02-28 | 北京天广实生物技术股份有限公司 | 结合人Claudin 18.2的抗体及其用途 |
WO2020160560A2 (en) * | 2019-02-01 | 2020-08-06 | Novarock Biotherapeutics, Ltd. | Anti-claudin 18 antibodies and methods of use thereof |
EP3959216A4 (en) * | 2019-04-24 | 2023-01-11 | Icahn School of Medicine at Mount Sinai | ANTI-NEURAMINIDASE ANTIBODIES TO INFLUENZA TYPE B VIRUS AND THEIR USES |
CA3139508A1 (en) | 2019-05-08 | 2020-11-12 | Janssen Biotech, Inc. | Materials and methods for modulating t cell mediated immunity |
CN111944048B (zh) * | 2019-05-16 | 2023-10-03 | 启愈生物技术(上海)有限公司 | 抗cldn抗体及其药物组合物和检测方法 |
WO2020228806A1 (zh) | 2019-05-16 | 2020-11-19 | 齐鲁制药有限公司 | 针对密蛋白18a2的抗体及其应用 |
CA3141504A1 (en) * | 2019-05-24 | 2020-12-03 | Sanyou Biopharmaceuticals Co., Ltd. | Novel cldn18.2 binding molecule |
AU2020332585A1 (en) * | 2019-08-20 | 2022-02-17 | Suzhou Transcenta Therapeutics Co., Ltd. | Novel anti-CLDN18.2 antibodies |
CN112409483B (zh) | 2019-08-22 | 2024-08-27 | 浙江道尔生物科技有限公司 | 抗pd-l1纳米抗体 |
CN112574307B (zh) * | 2019-09-29 | 2023-11-28 | 迈威(上海)生物科技股份有限公司 | 抗人Claudin18.2抗体及其应用 |
CN112707965A (zh) * | 2019-09-30 | 2021-04-27 | 和铂医药(苏州)有限公司 | 靶向cldn18.2的抗体及其制备方法和应用 |
CN115920078A (zh) * | 2019-11-05 | 2023-04-07 | 礼新医药科技(上海)有限公司 | 靶向紧密连接蛋白18.2的抗体药物偶联物 |
AU2020398045A1 (en) * | 2019-12-06 | 2022-06-09 | Sotio Biotech A.S. | Humanized CLDN18.2 antibodies |
KR20220127252A (ko) * | 2019-12-13 | 2022-09-19 | 알렉터 엘엘씨 | 항-mertk 항체 및 이의 사용 방법 |
CN114901365A (zh) | 2019-12-23 | 2022-08-12 | 斯迪安生物技术公司 | 肿瘤特异性密蛋白18.2抗体 |
CN118440202A (zh) * | 2019-12-27 | 2024-08-06 | 凯奥目生物科学株式会社 | 抗cdcp1抗体 |
US12060434B2 (en) * | 2020-02-25 | 2024-08-13 | Gensun Biopharma Inc. | Trispecific T cell engagers |
EP4110390A1 (en) * | 2020-02-27 | 2023-01-04 | Janssen Biotech, Inc. | Materials and methods for modulating an immune response |
BR112022019769A2 (pt) | 2020-03-30 | 2022-12-13 | BioNTech SE | Composições de rna que direcionam claudina-18.2 |
CN113493515B (zh) * | 2020-04-02 | 2023-03-28 | 广东菲鹏制药股份有限公司 | 抗cldn18a2的抗体以及治疗肿瘤的药物 |
CN115715202A (zh) * | 2020-05-15 | 2023-02-24 | 四川科伦博泰生物医药股份有限公司 | 抗体药物缀合物及其制备方法和用途 |
US20230331836A1 (en) * | 2020-05-25 | 2023-10-19 | Suzhou Transcenta Therapeutics Co., Ltd. | Anti-cldn18.2 antibodies and diagnostic uses thereof |
CN113735974B (zh) * | 2020-05-29 | 2023-10-27 | 杭州邦顺制药有限公司 | 针对Claudin18.2的抗体及其用途 |
US11976120B2 (en) | 2020-06-01 | 2024-05-07 | Boehringer Ingelheim International Gmbh | Antibodies targeting a complex comprising non-classical HLA-I and neoantigen and their methods of use |
US10981997B1 (en) | 2020-06-01 | 2021-04-20 | Abexxa Biologics, Inc. | Antibodies targeting a complex comprising non-classical HLA-I and neoantigen and their methods of use |
US10981996B1 (en) | 2020-06-01 | 2021-04-20 | Abexxa Biologics, Inc. | Antibodies targeting a complex comprising non-classical HLA-I and neoantigen and their methods of use |
CN113754778A (zh) * | 2020-06-05 | 2021-12-07 | 上海交通大学 | 靶向cldn18.2的嵌合抗原受体及其用途 |
CN111777681B (zh) * | 2020-07-06 | 2022-10-11 | 康诺亚生物医药科技(成都)有限公司 | 一种结合紧密连接蛋白-18.2的抗体及其用途 |
US20240059771A1 (en) | 2020-07-13 | 2024-02-22 | Shanghai Junshi Biosciences Co., Ltd. | Anti-cldn-18.2 antibody and use thereof |
CN111808194B (zh) * | 2020-07-13 | 2021-04-20 | 北京凯因科技股份有限公司 | 一种结合密蛋白的用于治疗癌症的人源化抗体 |
CN114222761B (zh) * | 2020-07-14 | 2024-02-20 | 浙江道尔生物科技有限公司 | 一种抗cld18a2的单域抗体 |
AU2021345124A1 (en) | 2020-09-16 | 2023-03-30 | Amgen Inc. | Methods for administering therapeutic doses of bispecific T-cell engaging molecules for the treatment of cancer |
CN114316046B (zh) * | 2020-09-29 | 2024-08-09 | 北京凯因科技股份有限公司 | 一种稳定的抗体组合物 |
UY39488A (es) | 2020-10-28 | 2022-04-29 | Janssen Biotech Inc | Composiciones y métodos para modular la inmunidad mediada por la cadena delta gamma |
KR20230104659A (ko) | 2020-11-08 | 2023-07-10 | 씨젠 인크. | 면역 세포 억제제를 이용한 조합-요법 항체 약물 접합체 |
CN112480248B (zh) | 2020-11-24 | 2023-05-05 | 三优生物医药(上海)有限公司 | 与cld18a2特异性结合的分子 |
WO2022122709A1 (en) | 2020-12-07 | 2022-06-16 | Sotio Biotech A.S. | Antibody-drug conjugates based on humanized cldn18.2 antibodies |
JP2024500242A (ja) | 2020-12-23 | 2024-01-05 | ソティオ バイオテック エイ.エス. | 腫瘍特異的クローディン18.2抗体と薬物との複合体 |
WO2022143794A1 (zh) | 2020-12-30 | 2022-07-07 | 百奥泰生物制药股份有限公司 | 抗cldn18.2抗体及其制备方法和应用 |
CN117460528A (zh) * | 2021-02-19 | 2024-01-26 | 苏州创胜医药集团有限公司 | 抗cldn18.2抗体缀合物 |
US20240182562A1 (en) | 2021-04-02 | 2024-06-06 | Oricell Therapeutics Co., Ltd | Cldn18.2 antigen-binding protein and use thereof |
WO2022226079A1 (en) * | 2021-04-20 | 2022-10-27 | Inbios International, Inc. | Neutralizing antibodies against sars-cov-2 |
WO2022253284A1 (zh) | 2021-06-02 | 2022-12-08 | 百奥泰生物制药股份有限公司 | 药物偶联物及其用途 |
JP2024523166A (ja) | 2021-06-15 | 2024-06-28 | ゼンコア インコーポレイテッド | クローディン18.2及びcd3に結合するヘテロ二量体抗体 |
WO2022262959A1 (en) | 2021-06-15 | 2022-12-22 | Astellas Pharma Europe Bv | Bispecific binding agents binding to cldn18.2 and cd3 |
EP4384204A1 (en) | 2021-08-13 | 2024-06-19 | Cytune Pharma | Il-2/il-15rbetagamma agonist combination with antibody-drug conjugates for treating cancer |
CN118159300A (zh) | 2021-09-27 | 2024-06-07 | 苏州信诺维医药科技股份有限公司 | 一种抗体及其药物偶联物和用途 |
WO2023161457A1 (en) | 2022-02-27 | 2023-08-31 | Evobright Gmbh | Bispecific antibodies against cd277 and a tumor-antigen |
WO2024074634A1 (en) | 2022-10-06 | 2024-04-11 | BioNTech SE | Rna compositions targeting claudin-18.2 |
WO2024074211A1 (en) | 2022-10-06 | 2024-04-11 | BioNTech SE | Rna compositions targeting claudin-18.2 |
CN115819586B (zh) * | 2022-10-13 | 2023-10-31 | 珠海市丽珠单抗生物技术有限公司 | 抗人SIRPα单克隆抗体及其用途 |
Family Cites Families (202)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3044382A (en) | 1957-12-14 | 1962-07-17 | Compur Werk Friedrich Deckel | Photographic shutter |
US4475196A (en) | 1981-03-06 | 1984-10-02 | Zor Clair G | Instrument for locating faults in aircraft passenger reading light and attendant call control system |
US4447233A (en) | 1981-04-10 | 1984-05-08 | Parker-Hannifin Corporation | Medication infusion pump |
US4474893A (en) | 1981-07-01 | 1984-10-02 | The University of Texas System Cancer Center | Recombinant monoclonal antibodies |
US4439196A (en) | 1982-03-18 | 1984-03-27 | Merck & Co., Inc. | Osmotic drug delivery system |
US4522811A (en) | 1982-07-08 | 1985-06-11 | Syntex (U.S.A.) Inc. | Serial injection of muramyldipeptides and liposomes enhances the anti-infective activity of muramyldipeptides |
US4447224A (en) | 1982-09-20 | 1984-05-08 | Infusaid Corporation | Variable flow implantable infusion apparatus |
US4487603A (en) | 1982-11-26 | 1984-12-11 | Cordis Corporation | Implantable microinfusion pump system |
US4486194A (en) | 1983-06-08 | 1984-12-04 | James Ferrara | Therapeutic device for administering medicaments through the skin |
US4596556A (en) | 1985-03-25 | 1986-06-24 | Bioject, Inc. | Hypodermic injection apparatus |
US5374548A (en) | 1986-05-02 | 1994-12-20 | Genentech, Inc. | Methods and compositions for the attachment of proteins to liposomes using a glycophospholipid anchor |
MX9203291A (es) | 1985-06-26 | 1992-08-01 | Liposome Co Inc | Metodo para acoplamiento de liposomas. |
GB8601597D0 (en) | 1986-01-23 | 1986-02-26 | Wilson R H | Nucleotide sequences |
US4954617A (en) | 1986-07-07 | 1990-09-04 | Trustees Of Dartmouth College | Monoclonal antibodies to FC receptors for immunoglobulin G on human mononuclear phagocytes |
US5260203A (en) | 1986-09-02 | 1993-11-09 | Enzon, Inc. | Single polypeptide chain binding molecules |
US4946778A (en) | 1987-09-21 | 1990-08-07 | Genex Corporation | Single polypeptide chain binding molecules |
US4881175A (en) | 1986-09-02 | 1989-11-14 | Genex Corporation | Computer based system and method for determining and displaying possible chemical structures for converting double- or multiple-chain polypeptides to single-chain polypeptides |
WO1988007089A1 (en) | 1987-03-18 | 1988-09-22 | Medical Research Council | Altered antibodies |
US5013653A (en) | 1987-03-20 | 1991-05-07 | Creative Biomolecules, Inc. | Product and process for introduction of a hinge region into a fusion protein to facilitate cleavage |
US5258498A (en) | 1987-05-21 | 1993-11-02 | Creative Biomolecules, Inc. | Polypeptide linkers for production of biosynthetic proteins |
US5091513A (en) | 1987-05-21 | 1992-02-25 | Creative Biomolecules, Inc. | Biosynthetic antibody binding sites |
DE3856559T2 (de) | 1987-05-21 | 2004-04-29 | Micromet Ag | Multifunktionelle Proteine mit vorbestimmter Zielsetzung |
US5132405A (en) | 1987-05-21 | 1992-07-21 | Creative Biomolecules, Inc. | Biosynthetic antibody binding sites |
US4790824A (en) | 1987-06-19 | 1988-12-13 | Bioject, Inc. | Non-invasive hypodermic injection device |
US4941880A (en) | 1987-06-19 | 1990-07-17 | Bioject, Inc. | Pre-filled ampule and non-invasive hypodermic injection device assembly |
GB8717430D0 (en) | 1987-07-23 | 1987-08-26 | Celltech Ltd | Recombinant dna product |
GB8809129D0 (en) | 1988-04-18 | 1988-05-18 | Celltech Ltd | Recombinant dna methods vectors and host cells |
US5108921A (en) | 1989-04-03 | 1992-04-28 | Purdue Research Foundation | Method for enhanced transmembrane transport of exogenous molecules |
US6020145A (en) * | 1989-06-30 | 2000-02-01 | Bristol-Myers Squibb Company | Methods for determining the presence of carcinoma using the antigen binding region of monoclonal antibody BR96 |
US5064413A (en) | 1989-11-09 | 1991-11-12 | Bioject, Inc. | Needleless hypodermic injection device |
US5312335A (en) | 1989-11-09 | 1994-05-17 | Bioject Inc. | Needleless hypodermic injection device |
JPH05504476A (ja) | 1989-12-27 | 1993-07-15 | アメリカ合衆国 | ヒト胃癌検出用診断プローブ |
US6255458B1 (en) | 1990-08-29 | 2001-07-03 | Genpharm International | High affinity human antibodies and human antibodies against digoxin |
GB9019812D0 (en) | 1990-09-11 | 1990-10-24 | Scotgen Ltd | Novel antibodies for treatment and prevention of infection in animals and man |
US5383851A (en) | 1992-07-24 | 1995-01-24 | Bioject Inc. | Needleless hypodermic injection device |
GB9223377D0 (en) | 1992-11-04 | 1992-12-23 | Medarex Inc | Humanized antibodies to fc receptors for immunoglobulin on human mononuclear phagocytes |
US5589579A (en) | 1994-07-19 | 1996-12-31 | Cytoclonal Pharmaceutics, Inc. | Gene sequence and probe for a marker of non-small cell lung carinoma |
US6121022A (en) | 1995-04-14 | 2000-09-19 | Genentech, Inc. | Altered polypeptides with increased half-life |
US5677139A (en) | 1995-04-21 | 1997-10-14 | President And Fellows Of Harvard College | In vitro differentiation of CD34+ progenitor cells into T lymphocytes |
UA56132C2 (uk) | 1995-04-25 | 2003-05-15 | Смітклайн Бічем Байолоджікалс С.А. | Композиція вакцини (варіанти), спосіб стабілізації qs21 відносно гідролізу (варіанти), спосіб приготування композиції вакцини |
AU728777B2 (en) | 1996-01-11 | 2001-01-18 | Corixa Corporation | Compositions and methods for the treatment and diagnosis of breast cancer |
WO2001049715A2 (en) | 2000-01-06 | 2001-07-12 | Genentech, Inc. | Methods and compositions for inhibiting neoplastic cell growth |
WO2000053756A2 (en) | 1999-03-08 | 2000-09-14 | Genentech, Inc. | Secreted and transmembrane polypeptides and nucleic acids encoding the same |
US6277375B1 (en) | 1997-03-03 | 2001-08-21 | Board Of Regents, The University Of Texas System | Immunoglobulin-like domains with increased half-lives |
US7411051B2 (en) | 1997-03-07 | 2008-08-12 | Human Genome Sciences, Inc. | Antibodies to HDPPA04 polypeptide |
WO2001054708A1 (en) | 2000-01-31 | 2001-08-02 | Human Genome Sciences, Inc. | 22 human secreted proteins |
US20070224663A1 (en) | 1997-03-07 | 2007-09-27 | Human Genome Sciences, Inc. | Human Secreted Proteins |
US7368531B2 (en) | 1997-03-07 | 2008-05-06 | Human Genome Sciences, Inc. | Human secreted proteins |
WO2000078961A1 (en) | 1999-06-23 | 2000-12-28 | Genentech, Inc. | Secreted and transmembrane polypeptides and nucleic acids encoding the same |
WO2000012708A2 (en) | 1998-09-01 | 2000-03-09 | Genentech, Inc. | Further pro polypeptides and sequences thereof |
US20030022298A1 (en) | 1997-09-15 | 2003-01-30 | Genentech, Inc. | Secreted and transmembrane polypeptides and nucleic acids encoding the same |
US20030073129A1 (en) | 1998-09-01 | 2003-04-17 | Genentech, Inc. | Secreted and transmembrane polypeptides and nucleic acids encoding the same |
US20020127584A1 (en) | 1997-09-18 | 2002-09-12 | Genentech, Inc. | Secreted and transmembrane polypeptides and nucleic acids encoding the same |
US20030008352A1 (en) | 1997-09-18 | 2003-01-09 | Genentech, Inc. | Secreted and transmembrane polypeptides and nucleic acids encoding the same |
US20030166104A1 (en) | 1997-09-18 | 2003-09-04 | Genentech, Inc. | Secreted and transmembrane polypeptides and nucleic acids encoding the same |
US20030027262A1 (en) | 1997-09-18 | 2003-02-06 | Genentech, Inc. | Secreted and transmembrane polypeptides and nucleic acids encoding the same |
US20050196832A1 (en) | 1997-09-18 | 2005-09-08 | Genentech, Inc. | Secreted and transmembrane polypeptides and nucleic acids encoding the same |
US20030027272A1 (en) | 1997-09-18 | 2003-02-06 | Genentech, Inc. | Secreted and transmembrane polypeptides and nucleic acids encoding the same |
US7160985B2 (en) | 1997-10-29 | 2007-01-09 | Genentech, Inc. | Pro180 polypeptide |
US6194551B1 (en) | 1998-04-02 | 2001-02-27 | Genentech, Inc. | Polypeptide variants |
US20030040471A1 (en) | 1998-04-29 | 2003-02-27 | Watson James D. | Compositions isolated from skin cells and methods for their use |
US20030022835A1 (en) | 1998-04-29 | 2003-01-30 | Genesis Research And Development Corporation Limited | Compositions isolated from skin cells and methods for their use |
JP3428441B2 (ja) | 1998-05-15 | 2003-07-22 | エーザイ株式会社 | タイトジャンクション構成膜蛋白質クローディンファミリー |
US7319008B2 (en) | 1998-06-02 | 2008-01-15 | Genentech, Inc. | Nucleic acid underexpressed in melanoma |
US7351543B2 (en) | 1998-06-02 | 2008-04-01 | Genentech, Inc. | Antibodies to a polypeptide encoded by a nucleic acid underexpressed in melanoma |
EP1084142A4 (en) | 1998-06-11 | 2005-01-19 | Smithkline Beecham Corp | GPR35A RECEIVER |
US7339033B2 (en) | 1998-06-26 | 2008-03-04 | Genentech, Inc. | Pro1481 |
EP1104486A4 (en) | 1998-08-04 | 2002-07-17 | Diadexus Llc | NEW METHOD FOR DIAGNOSIS, FOLLOW-UP, AND IMAGE OF LUNG CANCER |
US20050181478A1 (en) | 1998-09-01 | 2005-08-18 | Baker Kevin P. | Secreted and transmembrane polypeptides and nucleic acids encoding the same |
US20030082626A1 (en) | 1998-09-01 | 2003-05-01 | Genentech, Inc. | Secreted and transmembrane polypeptides and nucleic acids encoding the same |
US20030187191A1 (en) | 1998-09-01 | 2003-10-02 | Genentech, Inc. | Secreted and transmembrane polypeptides and nucleic acids encoding the same |
US7034123B2 (en) | 1998-09-01 | 2006-04-25 | Genetech, Inc. | Anti-PRO1347 antibodies |
CA2343577A1 (en) | 1998-09-16 | 2000-03-23 | Genentech, Inc. | Secreted and transmembrane polypeptides and nucleic acids encoding the same |
JP2002524103A (ja) | 1998-09-16 | 2002-08-06 | ザイモジェネティクス,インコーポレイティド | 胃ポリペプチドzsig28 |
JP2004500011A (ja) | 1998-10-06 | 2004-01-08 | キュラゲン コーポレイション | 新規な分泌タンパク質、およびそれをコードするポリヌクレオチド |
US7399834B2 (en) | 1998-10-07 | 2008-07-15 | Genentech, Inc. | Anti-PRO1558 antibodies |
US6235481B1 (en) | 1998-10-21 | 2001-05-22 | Arch Development Corporation & Board Of Regents | Polynucleotides encoding calpain 10 |
US20030187196A1 (en) | 1998-12-30 | 2003-10-02 | Genentech, Inc. | Secreted and transmembrane polypeptides and nucleic acids encoding the same |
US7026449B2 (en) | 1999-01-05 | 2006-04-11 | Genentech, Inc. | Secreted and transmembrane polypeptides and nucleic acids encoding the same |
US7507404B2 (en) | 1999-03-08 | 2009-03-24 | Genentech, Inc. | Secreted and transmembrane polypeptides and nucleic acids encoding the same |
KR100553300B1 (ko) | 1999-03-08 | 2006-02-20 | 제넨테크, 인크. | 혈관신생 및 심혈관형성의 촉진 또는 억제 방법 |
AU764092B2 (en) | 1999-03-23 | 2003-08-07 | Genentech Inc. | Secreted and transmembrane polypeptides and nucleic acids encoding the same |
JP2004507202A (ja) | 1999-03-31 | 2004-03-11 | キュラジェン コーポレイション | ポリペプチドをコードするオープンリーディングフレームを含む核酸;「orfx」 |
US20080286821A1 (en) | 1999-05-14 | 2008-11-20 | Eaton Dan L | Secreted and transmembrane polypeptides and nucleic acids encoding the same |
ATE357518T1 (de) | 1999-06-02 | 2007-04-15 | Genentech Inc | Verfahren und zusammensetzungen zur inhibierung des neoplastischen zellwachstums |
CA2383254A1 (en) | 1999-06-02 | 2000-12-07 | Genentech, Inc. | Secreted and transmembrane polypeptides and nucleic acids encoding the same |
AU3246100A (en) | 1999-06-02 | 2000-12-28 | Genentech Inc. | Methods and compositions for inhibiting neoplastic cell growth |
AU2215300A (en) | 1999-06-02 | 2000-12-28 | Genentech Inc. | Methods and compositions for inhibiting neoplastic cell growth |
CA2372511C (en) | 1999-06-15 | 2011-11-22 | Genentech, Inc. | Secreted and transmembrane polypeptides and nucleic acids encoding the same |
AU2883900A (en) | 1999-07-07 | 2001-01-30 | Genentech Inc. | Secreted and transmembrane polypeptides and nucleic acids encoding the same |
CA2380355A1 (en) | 1999-09-01 | 2001-03-08 | Genentech, Inc. | Secreted and transmembrane polypeptides and nucleic acids encoding the same |
AU1205901A (en) | 1999-10-14 | 2001-04-23 | Board Of Trustees Of The University Of Arkansas, The | Tumor antigen derived gene-16 (tadg-16): a novel extracellular serine protease and uses thereof |
CA2490909A1 (en) | 1999-12-01 | 2001-06-07 | Genentech, Inc. | Secreted and transmembrane polypeptides and nucleic acids encoding the same |
US6380362B1 (en) | 1999-12-23 | 2002-04-30 | Genesis Research & Development Corporation Ltd. | Polynucleotides, polypeptides expressed by the polynucleotides and methods for their use |
WO2001055326A2 (en) | 2000-01-31 | 2001-08-02 | Human Genome Sciences, Inc. | Nucleic acids, proteins, and antibodies |
US20040018969A1 (en) | 2000-01-31 | 2004-01-29 | Rosen Craig A. | Nucleic acids, proteins, and antibodies |
WO2001055208A1 (en) | 2000-01-31 | 2001-08-02 | Human Genome Sciences, Inc. | Nucleic acids, proteins, and antibodies |
AU2001247220A1 (en) | 2000-02-22 | 2001-09-03 | Corixa Corporation | Compositions and methods for diagnosis and therapy of malignant mesothelioma |
AU6802801A (en) | 2000-03-01 | 2001-09-24 | Genentech Inc | Secreted and transmembrane polypeptides and nucleic acids encoding the same |
WO2001070979A2 (en) | 2000-03-21 | 2001-09-27 | Millennium Pharmaceuticals, Inc. | Genes, compositions, kits, and method for identification, assessment, prevention and therapy of ovarian cancer |
US6436703B1 (en) | 2000-03-31 | 2002-08-20 | Hyseq, Inc. | Nucleic acids and polypeptides |
US6926898B2 (en) | 2000-04-12 | 2005-08-09 | Human Genome Sciences, Inc. | Albumin fusion proteins |
WO2001090357A1 (en) | 2000-05-24 | 2001-11-29 | Genesis Research & Development Corporation Limited | Compositions isolated from skin cells and methods for their use |
AU2001271589A1 (en) | 2000-06-30 | 2002-01-14 | Zymogenetics Inc. | Mammalian secreted proteins |
AU2001284703B2 (en) | 2000-08-03 | 2007-03-22 | Therapeutic Human Polyclonals Inc. | Production of humanized antibodies in transgenic animals |
JP2004519215A (ja) | 2000-08-15 | 2004-07-02 | イミュネックス・コーポレーション | クローディンポリペプチド |
JP2004512029A (ja) | 2000-08-16 | 2004-04-22 | カイロン コーポレイション | ヒト遺伝子および遺伝子発現産物 |
WO2002018576A2 (en) | 2000-08-28 | 2002-03-07 | Diadexus, Inc. | Compositions and methods relating to lung specific genes |
EP2298789B1 (en) | 2000-09-08 | 2012-03-14 | Schering Corporation | Mammalian genes; related reagents and methods |
US7829276B2 (en) | 2000-09-18 | 2010-11-09 | Thomas Jefferson University | Methods of using CRCA-1 as a stomach and esophageal cancer marker |
PT1354034E (pt) | 2000-11-30 | 2008-02-28 | Medarex Inc | Roedores transgénicos transcromossómicos para produção de anticorpos humanos |
WO2002061087A2 (en) | 2000-12-19 | 2002-08-08 | Lifespan Biosciences, Inc. | Antigenic peptides, such as for g protein-coupled receptors (gpcrs), antibodies thereto, and systems for identifying such antigenic peptides |
AU2002255478A1 (en) | 2001-01-10 | 2002-09-12 | Pe Corporation (Ny) | Kits, such as nucleic acid arrays, comprising a majority of human exons or transcripts, for detecting expression and other uses thereof |
US20030133939A1 (en) | 2001-01-17 | 2003-07-17 | Genecraft, Inc. | Binding domain-immunoglobulin fusion proteins |
US7754208B2 (en) | 2001-01-17 | 2010-07-13 | Trubion Pharmaceuticals, Inc. | Binding domain-immunoglobulin fusion proteins |
JP2004535776A (ja) | 2001-01-29 | 2004-12-02 | フェイズ − 1 モレキュラー トクシコロジー、インコーポレイテッド | ラット毒性関連遺伝子及びその使用 |
EP1412372A4 (en) | 2001-02-26 | 2005-08-24 | Arena Pharm Inc | ENDOGENOUS AND NON-ENDOGENOUS VERSIONS OF HUMAN G-PROTEIN COUPLED RECEPTORS |
US20030152939A1 (en) | 2001-04-09 | 2003-08-14 | Glennda Smithson | Novel secreted proteins and polynucleotides encoding them |
US20060084794A1 (en) | 2001-04-12 | 2006-04-20 | Human Genome Sciences, Inc. | Albumin fusion proteins |
JP2003000249A (ja) | 2001-05-10 | 2003-01-07 | Daiichi Fine Chemical Co Ltd | クローディンによるMT−MMPsを介したproMMP−2活性化 |
AU2002330714A1 (en) | 2001-05-30 | 2003-01-02 | Biomedical Center | In silico screening for phenotype-associated expressed sequences |
WO2003004604A2 (en) | 2001-07-06 | 2003-01-16 | Genentech, Inc. | Phage displayed pdz domain ligands |
CA2457424A1 (en) | 2001-08-03 | 2003-02-20 | Arbor Vita Corporation | Molecular interactions in cells |
US6551893B1 (en) | 2001-11-27 | 2003-04-22 | Micron Technology, Inc. | Atomic layer deposition of capacitor dielectric |
US20030018172A1 (en) | 2001-12-06 | 2003-01-23 | Genentech, Inc. | Secreted transmembrane polypeptides and nucleic acids encoding the same |
US20040002587A1 (en) | 2002-02-20 | 2004-01-01 | Watkins Jeffry D. | Fc region variants |
CA2379661A1 (en) | 2002-03-28 | 2003-09-28 | Kursad Turksen | Paracellular drug delivery system |
WO2003101283A2 (en) | 2002-06-04 | 2003-12-11 | Incyte Corporation | Diagnostics markers for lung cancer |
AU2003250367A1 (en) * | 2002-06-14 | 2003-12-31 | Immunomedics, Inc. | Monoclonal antibody pam4 and its use for diagnosis and therapy of pancreatic cancer |
EP3502133A1 (en) * | 2002-09-27 | 2019-06-26 | Xencor, Inc. | Optimized fc variants and methods for their generation |
MXPA05004022A (es) | 2002-10-17 | 2005-10-05 | Genmab As | Anticuerpos monoclonales humanos contra cd20. |
CA2505479A1 (en) | 2002-11-14 | 2004-06-03 | Arbor Vita Corporation | Molecular interactions in neurons |
DE10254601A1 (de) | 2002-11-22 | 2004-06-03 | Ganymed Pharmaceuticals Ag | Differentiell in Tumoren exprimierte Genprodukte und deren Verwendung |
EP1430902A1 (en) | 2002-12-20 | 2004-06-23 | Mondobiotech Laboratories Anstalt | Pharmaceutical composition of interferon gamma with molecular diagnostics for the improved treatment of asthma bronchiale |
EP2368578A1 (en) | 2003-01-09 | 2011-09-28 | Macrogenics, Inc. | Identification and engineering of antibodies with variant Fc regions and methods of using same |
US20050181375A1 (en) | 2003-01-10 | 2005-08-18 | Natasha Aziz | Novel methods of diagnosis of metastatic cancer, compositions and methods of screening for modulators of metastatic cancer |
US20060019256A1 (en) | 2003-06-09 | 2006-01-26 | The Regents Of The University Of Michigan | Compositions and methods for treating and diagnosing cancer |
CA2540894A1 (en) | 2003-10-03 | 2005-04-14 | Bayer Pharmaceuticals Corporation | Gene expression profiles and methods of use |
DE10354601B3 (de) | 2003-11-21 | 2005-06-23 | Chiropro Gmbh | Gelenkprothese für Fingerglieder |
WO2005052182A2 (en) | 2003-11-26 | 2005-06-09 | Yissum Research Development Company Of The Hebrew University Of Jerusalem | A method of analyzing plasma membrane protein content of cells |
US7858322B2 (en) | 2003-12-23 | 2010-12-28 | Nono, Inc. | Method of determining inhibition of binding to TRPM7 protein |
WO2005076939A2 (en) | 2004-02-09 | 2005-08-25 | University Of Kentucky Research Foundation | Assay and method for diagnosing and treating alzheimer’s disease |
WO2005082398A2 (en) | 2004-02-26 | 2005-09-09 | Ohio University | Diagnosis of hyperinsulinemia and type ii diabetes and protection against same based on genes differentially expressed in muscle cells |
US20050255041A1 (en) | 2004-05-13 | 2005-11-17 | Arius Research, Inc. | Cancerous disease modifying antibodies |
DE102004024617A1 (de) | 2004-05-18 | 2005-12-29 | Ganymed Pharmaceuticals Ag | Differentiell in Tumoren exprimierte Genprodukte und deren Verwendung |
EP2302394A1 (en) | 2004-05-21 | 2011-03-30 | The Institute for Systems Biology | Compositions and methods for quantification of serum glycoproteins |
WO2006023121A1 (en) | 2004-07-27 | 2006-03-02 | Ohio University | Diagnosis of hyperinsulinemia and type ii diabetes and protection against same based on genes differentially expressed in white adipose tissue (13) |
DE102004042822A1 (de) | 2004-08-31 | 2006-03-16 | Technische Universität Dresden | Verbindungen und Methoden zur Behandlung, Diagnose und Prognose bei Pankreaserkrankungen |
FR2876705B1 (fr) | 2004-10-19 | 2008-12-12 | Biomerieux Sa | Procede pour le diagnostic d'une intolerance a l'aspirine |
US20070072175A1 (en) | 2005-05-13 | 2007-03-29 | Biogen Idec Ma Inc. | Nucleotide array containing polynucleotide probes complementary to, or fragments of, cynomolgus monkey genes and the use thereof |
EP1910837B1 (en) | 2005-07-01 | 2012-03-14 | Arbor Vita Corporation | Methods and compositions for diagnosis and treatment of influenza |
JP2009504183A (ja) | 2005-08-15 | 2009-02-05 | ジェネンテック・インコーポレーテッド | 遺伝子破壊、それに関連する組成物および方法 |
EP2182057A1 (en) | 2005-08-31 | 2010-05-05 | Cell Signaling Technology, Inc. | Antibody agains phosphorylated Tyrosine for the detection of protein phosphorylation in carcinoma signaling pathways |
WO2007035690A2 (en) | 2005-09-19 | 2007-03-29 | Veridex, Llc | Methods for diagnosing pancreatic cancer |
AU2006304605A1 (en) | 2005-10-17 | 2007-04-26 | Institute For Systems Biology | Tissue-and serum-derived glycoproteins and methods of their use |
EP1790664A1 (en) | 2005-11-24 | 2007-05-30 | Ganymed Pharmaceuticals AG | Monoclonal antibodies against claudin-18 for treatment of cancer |
CN101448856A (zh) | 2006-03-29 | 2009-06-03 | 健泰科生物技术公司 | 肿瘤的诊断和治疗 |
WO2008013954A2 (en) | 2006-07-27 | 2008-01-31 | Cell Signaling Technology, Inc. | Tyrosine phosphorylation sites |
AU2007284651B2 (en) | 2006-08-09 | 2014-03-20 | Institute For Systems Biology | Organ-specific proteins and methods of their use |
WO2008021115A2 (en) | 2006-08-14 | 2008-02-21 | The Brigham And Women's Hospital, Inc. | Diagnostic tests using gene expression ratios |
KR20090071603A (ko) | 2006-09-19 | 2009-07-01 | 노파르티스 아게 | Raf 억제제에 대한 표적 조절, 효능, 진단 및/또는 예후의 바이오마커 |
SG166778A1 (en) | 2006-10-11 | 2010-12-29 | Max Planck Gesellschaft | Influenza targets |
EP2097538A4 (en) | 2006-12-07 | 2011-11-30 | Switchgear Genomics | TRANSCRIPTION REAGULATION ELEMENTS OF BIOLOGICAL PATHS, TOOLS AND METHODS |
EP2104734A2 (en) | 2006-12-08 | 2009-09-30 | Asuragen, INC. | Mir-20 regulated genes and pathways as targets for therapeutic intervention |
BRPI0807227A2 (pt) | 2007-02-01 | 2019-01-22 | Veridex Llc | métodos e materiais para identificação da origem de um carcinoma de origem primária desconhecida |
EP1983002A3 (en) | 2007-04-19 | 2009-03-11 | Peter Hornbeck | Tyrosine phosphorylation sites and antibodies specific for them |
EP1997832A1 (en) | 2007-05-29 | 2008-12-03 | Ganymed Pharmaceuticals AG | Monoclonal antibodies against Claudin-18 for treatment of cancer |
CA2689974A1 (en) | 2007-06-08 | 2008-12-18 | Asuragen, Inc. | Mir-34 regulated genes and pathways as targets for therapeutic intervention |
JPWO2008152822A1 (ja) | 2007-06-15 | 2010-08-26 | 株式会社メディネット | 医薬 |
US20100292303A1 (en) | 2007-07-20 | 2010-11-18 | Birrer Michael J | Gene expression profile for predicting ovarian cancer patient survival |
WO2009035497A2 (en) | 2007-08-08 | 2009-03-19 | Savidge Tor C | Disease related cysteine modifications and uses thereof |
EP2036987A1 (en) | 2007-09-17 | 2009-03-18 | Siemens Healthcare Diagnostics GmbH | Molecular markers for tumor cell content in tissue samples |
KR101528380B1 (ko) | 2007-09-19 | 2015-06-11 | 산토리 홀딩스 가부시키가이샤 | 세사민류와 아라키돈산류를 함유하는 조성물 |
JP2011501662A (ja) | 2007-10-12 | 2011-01-13 | ザ・プロウボウスト・フェロウズ・アンド・スカラーズ・オブ・ザ・カレッジ・オブ・ザ・ホリー・アンド・アンデバイデッド・トリニティ・オブ・クイーン・エリザベス・ニア・ダブリン | タイト結合を開放するための方法 |
WO2009102367A2 (en) | 2007-11-19 | 2009-08-20 | The Regents Of The University Of Colorado | Tight junction protein modulators and uses thereof |
KR20110018930A (ko) | 2008-06-02 | 2011-02-24 | 엔에스에이비피 파운데이션, 인크. | 암 치료에서 예후적 및 예견적 마커의 확인 및 용도 |
US20110190380A1 (en) | 2008-10-23 | 2011-08-04 | Elena Feinstein | Methods for delivery of sirna to bone marrow cells and uses thereof |
CN101381524A (zh) | 2008-10-24 | 2009-03-11 | 南开大学 | 单层氧化石墨与水溶性高分子增强复合材料 |
GB0904957D0 (en) | 2009-03-23 | 2009-05-06 | Univ Erasmus Medical Ct | Tumour gene profile |
WO2010120526A2 (en) | 2009-03-31 | 2010-10-21 | Emory University | Methods and systems for screening for and diagnosing dna methylation associated with autism spectrum disorders |
CN101584860A (zh) | 2009-04-27 | 2009-11-25 | 西安杰诺瓦生物科技有限公司 | 重组人Claudin18.2肿瘤疫苗及其制备方法 |
WO2010141093A2 (en) | 2009-06-04 | 2010-12-09 | The University Of Maryland, Baltimore | Co-signaling methods for treating cancers |
EP2483813A1 (en) | 2009-10-01 | 2012-08-08 | Chipdx LLC | System and method for classification of patients |
CN102858999A (zh) | 2009-12-01 | 2013-01-02 | 简要生物科学有限公司 | 癌症的分类 |
CA2786940C (en) | 2010-03-16 | 2019-09-24 | Biontech Ag | Tumor vaccination involving a humoral immune response, and proteins therefor including all or a portion of a hepatitis b virus core antigen protein and an epitope of claudin 18.2 |
EP2366709A1 (en) | 2010-03-16 | 2011-09-21 | BioNTech AG | Tumor vaccination involving a humoral immune response against self-proteins |
US8945847B2 (en) | 2010-05-24 | 2015-02-03 | Yissum Research Development Company Of The Hebrew University Of Jerusalem Ltd. | Methods and kits for ascertaining biosafety of an agent |
JP2013529089A (ja) | 2010-06-07 | 2013-07-18 | エフ.ホフマン−ラ ロシュ アーゲー | インターロイキン−6受容体を阻害するモノクローナル抗体による薬剤治療に対する応答を予測するための遺伝子発現マーカー |
US8454385B2 (en) | 2010-06-22 | 2013-06-04 | John Mezzalingua Associates, LLC | Coaxial cable connector with strain relief clamp |
WO2011163627A2 (en) | 2010-06-24 | 2011-12-29 | Integrated Diagnostics, Inc. | Organ specific diagnostic panels and methods for identification of organ specific panel proteins |
WO2012070014A2 (en) | 2010-11-26 | 2012-05-31 | Yissum Research Development Company Of The Hebrew University Of Jerusalem Ltd. | Identification of novel cell surface markers for pancreatic progenitor cells and definite endodermal cells |
CN103119180A (zh) | 2011-01-12 | 2013-05-22 | 森永乳业株式会社 | 产生具有免疫调节作用的乳的食物的筛选方法 |
DE102011005235B4 (de) | 2011-03-08 | 2017-05-24 | Sirs-Lab Gmbh | Verfahren zum Identifizieren einer Teilmenge von Polynucleotiden aus einer dem Humangenom entsprechenden Ausgangsmenge von Polynucleotiden zur in vitro Bestimmung eines Schweregrads der Wirtsantwort eines Patienten |
WO2013151664A1 (en) | 2012-04-02 | 2013-10-10 | modeRNA Therapeutics | Modified polynucleotides for the production of proteins |
WO2013167153A1 (en) | 2012-05-09 | 2013-11-14 | Ganymed Pharmaceuticals Ag | Antibodies useful in cancer diagnosis |
WO2013174404A1 (en) | 2012-05-23 | 2013-11-28 | Ganymed Pharmaceuticals Ag | Combination therapy involving antibodies against claudin 18.2 for treatment of cancer |
WO2013174403A1 (en) | 2012-05-23 | 2013-11-28 | Ganymed Pharmaceuticals Ag | Combination therapy involving antibodies against claudin 18.2 for treatment of cancer |
WO2014025198A2 (ko) | 2012-08-09 | 2014-02-13 | 주식회사 한독 | Lfa3 변이체 및 상기 변이체 또는 lfa3 cd2 결합영역과 이에 표적 특이적 폴리펩타이드가 연결된 융합단백질 및 그 용도 |
WO2014025199A2 (ko) | 2012-08-09 | 2014-02-13 | 주식회사 한독 | 스테필로코칼 엔테로톡신 유래의 초항원 변이체 및 이에 표적 특이적 폴리펩타이드가 연결된 융합단백질 및 그 용도 |
EP2888391A4 (en) | 2012-08-24 | 2016-09-14 | Univ Utah Res Found | COMPOSITIONS AND METHODS RELATING TO BLOOD BIOMARKERS OF BREAST CANCER |
US9856532B2 (en) | 2012-09-07 | 2018-01-02 | Institute For Systems Biology | Markers and methods for detecting posttraumatic stress disorder (PTSD) |
US20140073524A1 (en) | 2012-09-07 | 2014-03-13 | Institute For Systems Biology | Markers and methods for detecting posttraumatic stress disorder (ptsd) |
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